Polymorphism TaqIA Gen Dopamine D2 Receptor In Men Aged Start From 40 Years Old With Metabolic Syndrome Compared To Non Metabolic Syndrome

Muhammad Budi Syahputra
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Abstract

Introduction : Metabolic syndrome involves heritability , genetic , bad diet and lack of physical activity . One cause of the Metabolic Syndrome is a genetic abnormality in the dopamine D2 receptor gene that causes " Reward Deficiency Syndrome ". Aim: To investigate the relationship between polymorphisms of the dopamine D2 receptor gene Taq1A in men starting from 40 years of age with metabolic syndrome compared to those without metabolic syndrome. Methods: This research was done as an unpaired analytical research using case control design . The research subject is stored DNA isolates originating from metabolic syndrome 21 and 21 are non metabolic syndrome . Thermal Cycle process performed on isolates DNA using PCR techniques with applications located on a 310 bp band with a 2 % agarose gel , then the application in digestion with enzyme Taq1A ( New England Biolabs ®Inc ) and there are variant polymorphism ( T / C 310 bp , 180 bp , 130 bp ) , ( C / C 180 bp , 130 bp ) , ( T / T 310 bp ) and analyzed statistically using x² test , odds ratio. Result: Based on the metabolic syndrome X ² test was found genotype T / C at most ( 47.6 % ) , T / T ( 19.1 % ) , C / C ( 33.3 % ) with a value of p = 0.500 with a significance of p < 0 , 05 . In no metabolic syndrome T / C ( 61.9 % ) , T / T ( 9.5 % ) , C / C ( 28.6 % ) with a value of p = 0.457 with a significance of p < 0.05. Based on the distribution of allele no significant relationship. Conclusion: Based on the results of the study didn’t relate to the frequency distribution of genotype and allele distribution Taq1A polymorphisms of the dopamine D2 receptor gene in men aged from 40 years with the metabolic syndrome than those without metabolic syndrome
40岁以上男性代谢综合征患者与非代谢综合征患者TaqIA原多巴胺D2受体多态性
代谢综合征包括遗传性、遗传性、不良饮食和缺乏体育锻炼。代谢综合征的一个原因是多巴胺D2受体基因的遗传异常,导致“奖励缺乏综合征”。目的:探讨40岁以上男性代谢综合征患者与非代谢综合征患者多巴胺D2受体Taq1A基因多态性的关系。方法:采用病例对照设计进行非配对分析研究。研究对象是来源于代谢综合征21和非代谢综合征21的存储DNA分离株。热循环过程进行分离DNA使用PCR技术与应用程序位于310个基点乐队以2%琼脂糖凝胶,然后应用程序与酶消化Taq1A(新英格兰生物学实验室®Inc)有变体多态性(T / C 310个基点,180个基点,130个基点),(C / C 180个基点,130个基点),310个基点(T / T)和分析统计使用x²测试,比值比。结果:基于代谢综合征X²检验发现基因型T / C最多(47.6%),T / T最多(19.1%),C / C最多(33.3%),p = 0.500,差异有统计学意义p < 0.05。无代谢综合征患者T / C(61.9%)、T / T(9.5%)、C / C (28.6%), p = 0.457,差异有统计学意义,p < 0.05。基于等位基因的分布无显著关系。结论:基于本研究结果,40岁以上有代谢综合征男性多巴胺D2受体基因Taq1A多态性的基因型和等位基因分布频率分布与无代谢综合征男性不相关
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